ES335740A1 - Procedimiento para la obtencion de tetrahidrofurano. - Google Patents
Procedimiento para la obtencion de tetrahidrofurano.Info
- Publication number
- ES335740A1 ES335740A1 ES335740A ES335740A ES335740A1 ES 335740 A1 ES335740 A1 ES 335740A1 ES 335740 A ES335740 A ES 335740A ES 335740 A ES335740 A ES 335740A ES 335740 A1 ES335740 A1 ES 335740A1
- Authority
- ES
- Spain
- Prior art keywords
- phenyl
- piperidyl
- compound
- pyridyl
- reacting
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 150000001875 compounds Chemical class 0.000 abstract 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N Butanol Natural products CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 abstract 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical class C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 3
- -1 pyridyl compound Chemical class 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000005936 piperidyl group Chemical group 0.000 abstract 2
- 125000004076 pyridyl group Chemical group 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- FGEUIMWNIGSQPB-UHFFFAOYSA-N (4-methoxyphenyl)-pyridin-4-ylmethanone Chemical compound C1=CC(OC)=CC=C1C(=O)C1=CC=NC=C1 FGEUIMWNIGSQPB-UHFFFAOYSA-N 0.000 abstract 1
- PWOFVMNVYALSSU-UHFFFAOYSA-N 1-[4-[2-(4-chlorophenyl)oxolan-2-yl]piperidin-1-yl]ethanone Chemical compound ClC1=CC=C(C=C1)C1(OCCC1)C1CCN(CC1)C(C)=O PWOFVMNVYALSSU-UHFFFAOYSA-N 0.000 abstract 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 abstract 1
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 abstract 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract 1
- ZOPKGHOTDFOYNE-UHFFFAOYSA-N 4-[2-(4-chlorophenyl)oxolan-2-yl]piperidine Chemical compound C1=CC(Cl)=CC=C1C1(C2CCNCC2)OCCC1 ZOPKGHOTDFOYNE-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 239000002168 alkylating agent Substances 0.000 abstract 1
- 229940100198 alkylating agent Drugs 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 235000019253 formic acid Nutrition 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 238000007327 hydrogenolysis reaction Methods 0.000 abstract 1
- 238000010348 incorporation Methods 0.000 abstract 1
- RBWRWAUAVRMBAC-UHFFFAOYSA-M magnesium;methoxybenzene;bromide Chemical compound [Mg+2].[Br-].COC1=CC=[C-]C=C1 RBWRWAUAVRMBAC-UHFFFAOYSA-M 0.000 abstract 1
- SKFLCXNDKRUHTA-UHFFFAOYSA-N phenyl(pyridin-4-yl)methanone Chemical compound C=1C=NC=CC=1C(=O)C1=CC=CC=C1 SKFLCXNDKRUHTA-UHFFFAOYSA-N 0.000 abstract 1
- 150000003053 piperidines Chemical class 0.000 abstract 1
- GPHQHTOMRSGBNZ-UHFFFAOYSA-N pyridine-4-carbonitrile Chemical compound N#CC1=CC=NC=C1 GPHQHTOMRSGBNZ-UHFFFAOYSA-N 0.000 abstract 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 1
- 230000001225 therapeutic effect Effects 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH70266 | 1966-01-19 | ||
| CH1763566 | 1966-12-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES335740A1 true ES335740A1 (es) | 1968-03-16 |
Family
ID=25685421
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES335740A Expired ES335740A1 (es) | 1966-01-19 | 1967-01-17 | Procedimiento para la obtencion de tetrahidrofurano. |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3488356A (is") |
| AT (4) | AT266105B (is") |
| BE (1) | BE692810A (is") |
| ES (1) | ES335740A1 (is") |
| FR (1) | FR1513600A (is") |
| GB (1) | GB1133302A (is") |
| NL (1) | NL6700808A (is") |
| OA (1) | OA02303A (is") |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1186192A (fr) * | 1957-02-26 | 1959-08-17 | Rhone Poulenc Sa | Nouveaux pipéridyl-2 dioxolannes et leur préparation |
| US2971003A (en) * | 1959-11-16 | 1961-02-07 | Frosst & Co Charles E | 2, 2-dialkyl-4-(pyridyl ethyl)-tetrahydrofuran-4-methyl carbamate |
-
1967
- 1967-01-10 US US608277A patent/US3488356A/en not_active Expired - Lifetime
- 1967-01-12 FR FR90814A patent/FR1513600A/fr not_active Expired
- 1967-01-16 GB GB2135/67A patent/GB1133302A/en not_active Expired
- 1967-01-17 ES ES335740A patent/ES335740A1/es not_active Expired
- 1967-01-18 AT AT50067A patent/AT266105B/de active
- 1967-01-18 NL NL6700808A patent/NL6700808A/xx unknown
- 1967-01-18 BE BE692810D patent/BE692810A/xx unknown
- 1967-01-18 OA OA52726A patent/OA02303A/xx unknown
- 1967-01-18 AT AT1063567A patent/AT269125B/de active
- 1967-01-18 AT AT1063367A patent/AT269124B/de active
- 1967-01-18 AT AT1063667A patent/AT269858B/de active
Also Published As
| Publication number | Publication date |
|---|---|
| BE692810A (is") | 1967-07-18 |
| US3488356A (en) | 1970-01-06 |
| GB1133302A (en) | 1968-11-13 |
| AT269858B (de) | 1969-04-10 |
| AT266105B (de) | 1968-11-11 |
| OA02303A (fr) | 1970-05-05 |
| FR1513600A (fr) | 1968-02-16 |
| NL6700808A (is") | 1967-07-20 |
| AT269124B (de) | 1969-03-10 |
| AT269125B (de) | 1969-03-10 |
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